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Kit for determining glycated serum proteins and preparation method of kit

A technology of glycosylated serum protein and a kit, which is applied in the field of kits for measuring glycosylated serum protein and its preparation, can solve problems such as radioactive contamination by radiochemical methods, complex operation of gas chromatography, and poor stability of reagents, and achieve detection results Accurate, stable colored substances, easy to operate effect

Inactive Publication Date: 2016-07-27
ANHUI IPROCOM BIOTECH CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The technical problem to be solved by the present invention is to provide a test kit for the determination of glycosylated serum protein in order to overcome the defects of radiochemical method with radioactive pollution, gas chromatography with complicated operation and long time consumption, and enzymatic method with poor reagent stability and its preparation method

Method used

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  • Kit for determining glycated serum proteins and preparation method of kit

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0064] The test kit of the present invention includes reagent R1 and reagent R2 two-liquid components independent of each other, wherein

[0065] Reagent R1:

[0066] Potassium phosphate buffer 50mmol / L

[0067] Calcium chloride 100mmol / L

[0068] Uricase 6KU / L

[0069] Ascorbate oxidase 14KU / L

[0070] Alkyl glucoside 7.0g / L

[0071] TritonX-1000.5mmol / L

[0072] Sodium azide 0.05g / L

[0073] Its solvent is purified water.

[0074] Reagent R2:

[0075] Potassium phosphate buffer 50mmol / L

[0076] Tetrazolium blue 0.9mmol / L

[0077] Sodium azide 0.05g / L

[0078] Its solvent is purified water.

Embodiment 2

[0080] The test kit of the present invention includes reagent R1 and reagent R2 two-liquid components independent of each other, wherein

[0081] Reagent R1:

[0082] Potassium phosphate buffer 90mmol / L

[0083] Calcium chloride 50mmol / L

[0084] Uricase 9KU / L

[0085] Ascorbate oxidase 18KU / L

[0086] Alkyl glucoside 12.0g / L

[0087] TritonX-1000.3mmol / L

[0088] Sodium azide 0.09g / L

[0089] Its solvent is purified water.

[0090] Reagent R2:

[0091]Potassium phosphate buffer 90mmol / L

[0092] Tetrazolium blue 1.5mmol / L

[0093] Sodium azide 0.01g / L

[0094] Its solvent is purified water.

Embodiment 3

[0096] Kit preparation and method of use

[0097] 1. Prepare the reagent according to the content of the following components:

[0098] Reagent R1:

[0099] Potassium phosphate buffer 50mmol / L

[0100] Calcium chloride 100mmol / L

[0101] Uricase 6KU / L

[0102] Ascorbate oxidase 14KU / L

[0103] Alkyl glucoside 7.0g / L

[0104] TritonX-1000.5mmol / L

[0105] Sodium azide 0.05g / L

[0106] Its solvent is purified water.

[0107] Reagent R2:

[0108] Potassium phosphate buffer 50mmol / L

[0109] Tetrazolium blue 0.9mmol / L

[0110] Sodium azide 0.05g / L

[0111] Its solvent is purified water.

[0112] 2. Parameter setting of automatic biochemical analyzer

[0113] (a) Detection temperature: 37°C;

[0114] (b) Detection wavelength: main wavelength 546nm, secondary wavelength 700nm;

[0115] (c) Reaction time: 10 minutes, among which, the incubation time is 5 minutes, measure and read the absorbance A1 immediately after adding the reagent R2, and read the absorbance A2 af...

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Abstract

The invention discloses a kit for determining glycated serum proteins and a preparation method of the kit. The kit comprises two liquid components of a reagent R1 and a reagent R2 which are independent from each other, and comprises the following components of the following content: the reagent R1: 10 to 90 mmol / L of potassium phosphate buffer solution, 50 to 250 mmol / L of calcium chloride, 3 to 9 KU / L of uricase, 10 to 18 KU / L of ascorbic acid oxidase, 2.0 to 12.0 g / L of alkyl glycoside, 0.3 to 0.7 mmol / L of TritonX-100, 0.01 to 0.09 g / L of sodium azide, and a solvent of the reagent R1 is purified water; the reagent R2: 10 to 90 mmol / L of potassium phosphate buffer solution, 0.3 to 1.5 mmol / L of blue tetrazolium, 0.01 to 0.09 g / L of sodium azide, and a solvent of the reagent R2 is purified water. The preparation method comprises the following steps: preparing the reagents according to the component content; mixing a sample to be detected, the reagent R1 and the reagent R2, and enabling the mixture to sufficiently react; determining an absorbance difference value after the reaction by utilizing a full-automatic biochemical analyzer; calculating the concentration of the glycated serum proteins in the sample according to an absorbance variation value. The kit has the advantages of high accuracy, no pollution and the like.

Description

technical field [0001] The invention relates to the technical fields of medicine and biochemistry, in particular to a kit for measuring glycosylated serum protein and a preparation method thereof. Background technique [0002] Glucose in the blood undergoes a non-enzymatic glycation reaction with the N-terminus of albumin and other protein molecules to form glycated serum proteins. The glycation of serum proteins mainly occurs on the lysine residues of protein molecules, of which albumin is the main one, and glycated serum The half-life of protein (GSP) is 17-19 days. The measurement of glycosylated serum protein (GSP) can reflect the average blood sugar level of 2-3 weeks before the measurement, and is not affected by the blood sugar concentration at that time. It is a good indicator for monitoring blood sugar in diabetic patients. Therefore, the determination of glycosylated serum protein is of great significance in the diagnosis, short-term monitoring and efficacy evaluat...

Claims

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Application Information

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IPC IPC(8): G01N21/78
CPCG01N21/78G01N2021/775
Inventor 蔡晓辉庄庆华吴铮徐运
Owner ANHUI IPROCOM BIOTECH CO LTD
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